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利用基于 CRISPR-Cas12a 的检测方法快速检测和追踪 SARS-CoV-2 的奥密克戎变异株。

Rapid detection and tracking of Omicron variant of SARS-CoV-2 using CRISPR-Cas12a-based assay.

机构信息

Department of Epidemiology, School of Public Health, Southern Medical University, Guangzhou, 510515, China.

Institute of Pathogenic Microbiology, Guangdong Provincial Center for Disease Control and Prevention, Guangdong Workstation for Emerging Infectious Disease Control and Prevention, Chinese Academy of Medical Sciences, Guangzhou, 511430, China.

出版信息

Biosens Bioelectron. 2022 Jun 1;205:114098. doi: 10.1016/j.bios.2022.114098. Epub 2022 Feb 17.

Abstract

BACKGROUND

The newly emerged SARS-CoV-2 variant of concern (VOC) Omicron is spreading quickly worldwide, which manifests an urgent need of simple and rapid assay to detect and diagnose Omicron infection and track its spread.

METHODS

To design allele-specific CRISPR RNAs (crRNAs) targeting the signature mutations in the spike protein of Omicron variant, and to develop a CRISPR-Cas12a-based assay to specifically detect Omicron variant.

RESULTS

Our system showed a low limit of detection of 2 copies per reaction for the plasmid DNA of Omicron variant, and could readily detect Omicron variant in 5 laboratory-confirmed clinical samples and distinguish them from 57 SARS-CoV-2 positive clinical samples (4 virus isolates and 53 oropharyngeal swab specimens) infected with wild-type (N = 8) and the variants of Alpha (N = 17), Beta (N = 17) and Delta (N = 15). The testing results could be measured by fluorescent detector or judged by naked eyes. In addition, no cross-reaction was observed when detecting 16 clinical samples infected with 9 common respiratory pathogens.

CONCLUSIONS

The rapid assay could be easily set up in laboratories already conducting SARS-CoV-2 nucleic acid amplification tests and implemented routinely in resource-limited settings to monitor and track the spread of Omicron variant.

摘要

背景

新出现的关注变异株(VOC)奥密克戎在全球迅速传播,这迫切需要一种简单、快速的检测方法来检测和诊断奥密克戎感染,并追踪其传播。

方法

针对奥密克戎变异株刺突蛋白中的特征性突变设计靶向特异性 CRISPR RNA(crRNA),并开发基于 CRISPR-Cas12a 的检测方法来特异性检测奥密克戎变异株。

结果

我们的系统对奥密克戎变异株的质粒 DNA 的检测下限低至每个反应 2 个拷贝,并且可以在 5 个实验室确诊的临床样本中轻易检测到奥密克戎变异株,并将其与 57 个 SARS-CoV-2 阳性临床样本(4 个病毒分离株和 53 个或咽拭子标本)区分开来,这些样本感染了野生型(N=8)和阿尔法(N=17)、贝塔(N=17)和德尔塔(N=15)变异株。检测结果可以通过荧光检测仪测量或肉眼判断。此外,在检测 16 个感染了 9 种常见呼吸道病原体的临床样本时,未观察到交叉反应。

结论

该快速检测方法可在已开展 SARS-CoV-2 核酸扩增检测的实验室中轻松建立,并在资源有限的环境中常规实施,以监测和追踪奥密克戎变异株的传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7e2/8849905/47b2f72e23f1/gr1_lrg.jpg

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